SIST EN 12470-1:2000/kprA1:2009

Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device

Medizinische Thermometer - Teil 1: Mit metallischer Flüssigkeit gefüllte Glasthermometer mit Maximumvorrichtung

Thermomètres médicaux - Partie 1: Thermomètres à dilatation de liquide métallique dans une gaine de verre, avec dispositif à maximum

Klinični termometri - 1. del: Zaprti stekleni termometri s tekočimi kovinami

General Information

• Status: Not Published
• Public Enquiry End Date: 09-Apr-2009
• ICS: 11.040.55 - Diagnostic equipment
• Technical Committee: VAZ - Healthcare
• Current Stage: 98 - Abandoned project (Adopted Project)
• Start Date: 27-Mar-2013
• Due Date: 01-Apr-2013
• Completion Date: 27-Mar-2013
• Directive: 2007/47/EC - Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market
• Directive: 93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Mandate: M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
• Ref Project: EN 12470-1:2000/prA1 - Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device

Relations

• Amends: SIST EN 12470-1:2000 - Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device
• Effective Date: 01-Apr-2009
• Consolidated By: SIST EN 12470-1:2000+A1:2009 - Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device
• Effective Date: 18-Jan-2023
• Consolidated By: SIST EN 12470-1:2000+A1:2009 - Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device
• Effective Date: 19-Jan-2023
• Consolidated By: SIST EN 12470-1:2000+A1:2009 - Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device
• Effective Date: 01-Oct-2009

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 12470-1:2000/kprA1:2009
01-april-2009
.OLQLþQLWHUPRPHWULGHO=DSUWLVWHNOHQLWHUPRPHWULVWHNRþLPLNRYLQDPL
Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum
device
Medizinische Thermometer - Teil 1: Mit metallischer Flüssigkeit gefüllte Glasthermometer
mit Maximumvorrichtung
Thermomètres médicaux - Partie 1: Thermomètres à dilatation de liquide métallique dans
une gaine de verre, avec dispositif à maximum
Ta slovenski standard je istoveten z: EN 12470-1:2000/prA1
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
SIST EN 12470-1:2000/kprA1:2009 en,fr
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 12470-1:2000/kprA1:2009

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SIST EN 12470-1:2000/kprA1:2009
EUROPEAN STANDARD
FINAL DRAFT
EN 12470-1:2000
NORME EUROPÉENNE
EUROPÄISCHE NORM
prA1
January 2009
ICS 17.200.20

English Version
Clinical thermometers - Part 1: Metallic liquid-in-glass
thermometers with maximum device
Thermomètres médicaux - Partie 1: Thermomètres à Medizinische Thermometer - Teil 1: Mit metallischer
dilatation de liquide métallique dans une gaine de verre, Flüssigkeit gefüllte Glasthermometer mit
avec dispositif à maximum Maximumvorrichtung
This draft amendment is submitted to CEN members for unique acceptance procedure. It has been drawn up by the Technical Committee
CEN/TC 205.
This draft amendment A1, if approved, will modify the European Standard EN 12470-1:2000. If this draft becomes an amendment, CEN
members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of this amendment
into the relevant national standard without any alteration.
This draft amendment was established by CEN in three official versions (English, French, German). A version in any other language made
by translation under the responsibility of a CEN member into its own language and notified to the CEN Management Centre has the same
status as the official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia, Finland,
France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal,
Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without notice and
shall not be referred to as a European Standard.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2009 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN 12470-1:2000/prA1:2009: E
worldwide for CEN national Members.

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SIST EN 12470-1:2000/kprA1:2009
EN 12470-1:2000/prA1:2009 (E)
Contents Page
Foreword .3
1 Modification to 8.1, General .4
2 Modification to 8.2, Marking .4
3 Modification to 8.3, Instructions for use.4
4 Modification to Annex ZA .4

2

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SIST EN 12470-1:2000/kprA1:2009
EN 12470-1:2000/prA1:2009 (E)
Foreword
This document (EN 12470-1:2000/prA1:2009) has been prepared by Technical Committee CEN/TC 205 “Non-
active medical devices”, the secretariat of which is held by DIN.
This document is currently submitted to the Unique Acceptance Procedure.
This document has been prepared un
...